FALSELY NORMAL VALUE IN FLUOROMETRIC TRANSFERASE SCREENING OF GALACTOSEMIC BLOOD. A CAUTIONARY NOTEBEUTLER E; GELBART T.1981; AM. J. CLIN. PATHOL.; ISSN 0002-9173; USA; DA. 1981; VOL. 76; NO 6; PP. 841-842; BIBL. 5 REF.Article

Plasma glutathione in health and in patients with malignant diseaseBEUTLER, E; GELBART, T.The Journal of laboratory and clinical medicine. 1985, Vol 105, Num 5, pp 581-584, issn 0022-2143Article

Two new Gaucher disease mutationsBEUTLER, E; GELBART, T.Human genetics. 1994, Vol 93, Num 2, pp 209-210, issn 0340-6717Article

Gaucher disease associated with a unique KpnI restriction site : identification of the amino-acid substitutionBEUTLER, E; GELBART, T.Annals of human genetics. 1990, Vol 54, Num 2, pp 149-153, issn 0003-4800, 5 p.Article

The mechanism of removal of leukocytes by cellulose columnsBEUTLER, E; GELBART, T.Blood cells. 1986, Vol 12, Num 1, pp 57-64, issn 0340-4684Conference Paper

Gaucher disease mutations in non-Jewish patientsBEUTLER, E; GELBART, T.British journal of haematology. 1993, Vol 85, Num 2, pp 401-405, issn 0007-1048Article

Improved assay of the enzymes of glutathione synthesis: γ-glutamylcysteine synthetase and glutathione synthetaseBEUTLER, E; GELBART, T.Clinica chimica acta. 1986, Vol 158, Num 1, pp 115-123, issn 0009-8981Article

THE EFFECTS ON OXYGEN AFFINITY AND GELATION OF HEMOGLOBIN S CROSSLINKED BY REACTION WITH METHYL ACETIMIDATECHAO TL; BERENFELD MR; GELBART T et al.1981; HEMOGLOBIN; USA; DA. 1981; VOL. 5; NO 1; PP. 47-72; BIBL. 2 P.Article

IN VIVO SURVIVAL STUDIES OF ⁵¹CR-LABELED METHYL ACETIMIDATE TREATED ERYTHROCYTES IN PATIENTS WITH SICKLE CELL DISEASEGABUZDA TG; CHAO TL; BERENFELD MR et al.1980; BLOOD; ISSN 0006-4971; USA; DA. 1980; VOL. 56; NO 6; PP. 1041-1047; BIBL. 21 REF.Article

The facile detection of tht nt 1226 mutation of glucoerebrosidase by mismatched PCRBEUTLER, E; GELBART, T; WEST, C et al.Clinica chimica acta. 1990, Vol 194, Num 2-3, pp 161-166, issn 0009-8981, 6 p.Article

A previously undescribed nonsense mutation of the HFE geneBEUTLER, E; GRIFFIN, M. J; GELBART, T et al.Clinical genetics. 2002, Vol 61, Num 1, pp 40-42, issn 0009-9163Article

Evolution of the genome and the genetic code: selection at the dinucleotide level by methylation and polyribonucleotide cleavageBEUTLER, E; GELBART, T; JIAHUAI HAN et al.Proceedings of the National Academy of Sciences of the United States of America. 1989, Vol 86, Num 1, pp 192-196, issn 0027-8424Article

The effect of HFE genotypes on measurements of iron overload in patients attending a Health appraisal clinicBEUTLER, E; FELITTI, V; GELBART, T et al.Annals of internal medicine. 2000, Vol 133, Num 5, pp 329-337, issn 0003-4819Article

Interference of heparin with the polymerase chain reactionBEUTLER, E; GELBART, T; KUHL, W et al.BioTechniques. 1990, Vol 9, Num 2, issn 0736-6205, p. 166Article

Triose phosphate isomerase deficiency in 3 French families : two novel null alleles, a frameshift mutation (TPI Alfortville) and an alteration in the initiation codon (TPI Paris)VALENTIN, C; PISSARD, S; COHEN-SOLAL, M et al.Blood. 2000, Vol 96, Num 3, pp 1130-1135, issn 0006-4971Article

Three genes encoding zinc finger proteins on human chromosome 6p21.3 : Members of a new subclass of the Krüppel gene family containing the conserved SCAN box domainLEE, P. L; GELBART, T; WEST, C et al.Genomics (San Diego, Calif.). 1997, Vol 43, Num 2, pp 191-201, issn 0888-7543Article

G-6-PD Walter Reed: possible insight into structural NADP in G-6-PDBEUTLER, E; HARTMAN, K; GELBART, T et al.American journal of hematology. 1986, Vol 23, Num 1, pp 25-30, issn 0361-8609Article

Chronic granulomatous disease and glutathione peroxidase deficiency, revisitedNEWBURGER, P. E; MALAWISTA, S. E; DINAUER, M. C et al.Blood. 1994, Vol 84, Num 11, pp 3861-3869, issn 0006-4971Article

Gamma-glutamylcysteine synthetase deficiency and hemolytic anemiaBEUTLER, E; MOROOSE, R; KRAMER, L et al.Blood. 1990, Vol 75, Num 1, pp 271-273, issn 0006-4971Article

Tight linkage of pyruvate kinase (PKLR) and glucocerebrosidase (GBA) genesGLENN, D; GELBART, T; BEUTLER, E et al.Human genetics. 1994, Vol 93, Num 6, pp 635-638, issn 0340-6717Article

Human red cell glucose-6-phosphate dehydrogenase : all active enzyme has sequence predicted by the × chromosome-encoded cDNABEUTLER, E; GELBART, T; KUHL, W et al.Cell (Cambridge). 1990, Vol 62, Num 1, pp 7-8, issn 0092-8674, 2 p.Article

6-phosphogluconolactonase deficiency, a hereditary erythrocyte enzyme deficiency: possible interaction with glucose-6-phosphate dehydrogenase deficiencyBEUTLER, E; KUHL, W; GELBART, T et al.Proceedings of the National Academy of Sciences of the United States of America. 1985, Vol 82, Num 11, pp 3876-3878, issn 0027-8424Article

Mechanism of improved maintenance of 2,3-diphosphoglycerate in stored blood by the xanthone compound 2-(2-hydroxyethoxy)-6-(1-H-tetrazole-5-yl)xanthen-9-one (BW A440C)BEUTLER, E; FORMAN, L; WEST, C et al.Biochemical pharmacology. 1988, Vol 37, Num 6, pp 1057-1060, issn 0006-2952Article

Identification of six new Gaucher disease mutationsBEUTLER, E; GELBART, T; WEST, C et al.Genomics (San Diego, Calif.). 1993, Vol 15, Num 1, pp 203-205, issn 0888-7543Article

Polymorphisms in the human glucocerebrosidase geneBEUTLER, E; WEST, C; GELBART, T et al.Genomics (San Diego, Calif.). 1992, Vol 12, Num 4, pp 795-800, issn 0888-7543Article